Preparation method for molecular recognition sensor by electrodeposition
a molecular recognition and sensor technology, applied in the field of preparation of molecular recognition sensors by electrodeposition, can solve the problems of high production cost, short shelf life, stringent environmental requirements, etc., and achieve the effects of low cost, and simple and controllable preparation
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example 1
(1) Preparation of Ionic Photosensitive Copolymer
[0043]Synthesis of ionic photosensitive copolymer (4-vinyl pyridine-co-acrylic acid-co-(2-hydroxymethyl-(4-methyl coumarin)oxyethyl-methyl acrylate)), abbreviated as P(4VP-co-AA-co-CGMA). 0.525 g (0.005 mol) 4-vinylpyridine, 0.36 g (0.005 mol) acrylic acid, 3.18 g (0.01 mol) 2-hydroxymethyl-(4-methyl coumarin) ethyl-methyl acrylate, and 0.049 g (0.3 mmol, 1.5% of the total molar weight of monomers) azodiisobutyronitrile as initiator were dissolved in 25 mL dioxane. The mixture was degassed with nitrogen gas for 20 min and sealed under vacuum, then placed in a preheated oil bath (70° C.) for 12 hours under stirring. The resultant polymers were purified by reprecipitation three times into mixed solvents of methanol and water (8:2 in volume ratio) and then dried under vacuum at 30° C.
(2) Preparation of Molecularly Imprinted Polymeric Micelles
[0044]The obtained copolymers were dissolved in dimethyl sulfoxide to get solution with a solid c...
example 2
(1) Preparation of the Ionic Photosensitive Copolymer
[0046]Synthesis of poly(maleic anhydride-co-styrene-co-(7-(4-vinyl benzyloxy)-4-methylcoumarin), abbreviated as P(Man-co-St-co-VM). 2.352 g (0.024 mol) maleic anhydride, 1.56 g (0.015 mol) styrene, 1.46 g (0.005 mol) 7-(4-vinyl benzyloxy)-4-methylcoumarin, and the initiator 0.072 g (0.44 mmol) azodiisobutyronitrile were dissolved in 25 mL dioxane and added into flask. The mixture was degassed with nitrogen gas for 50 min and sealed under vacuum, then placed in a preheated oil bath (65° C.) for 8 hours under stirring. The resultant polymers were purified by reprecipitation three times into mixed solvents of methanol and water (8:2 in volume ratio) and then dried under vacuum at 30° C. The resultant polymer was dissolved in DMF and then added dropwise with alkaline aqueous solution. The resultant solution was heated to 90° C. to hydrolyze the maleic anhydride. The ionic photosensitive copolymers were obtained after dialysis and free...
example 3
(1) Preparation of Ionic Photosensitive Copolymer
[0049]Synthesis of amphiphilic poly((2,4-diamino-6-vinyl-S-triazine)-co-methylacrylic poly(ethylene glycol) ester-co-(2-cinnamic acyloxyethyl methylacrylate)), abbreviated as P(VDAT-co-MPEG-co-CEMA). 2.74 g (0.02 mol) 2,4-diamino-6-vinyl-S-triazine, 4.75 g (0.01 mol) methylacrylic poly(ethylene glycol) ester, 2.46 g (0.01 mol) 2-cinnamic acyloxyethyl methylacrylate, and the initiator 0.099 g azodiisobutyronitrile were dissolved into 25 mL dioxane and added into flask. The mixture was degassed with nitrogen gas for 50 min and sealed under vacuum, then placed in a preheated oil bath (65° C.) for 8 hours under stirring. The resultant polymers were purified by reprecipitation three times into mixed solvents of methanol and water (1:1 in volume ratio) and then dried under vacuum at 30° C.
(2) Preparation of Molecularly Imprinted Polymeric Micelles
[0050]The obtained polymers were dissolved in DMF and uracil was then added as the template mol...
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